[0001] The present invention pertains to the iron and steel industry and may be used in
out-of-furnace treatment (secondary treatment) (metallurgy) of molten irons and steels,
including in particular, for deoxidizing, desulfurizing and modifying iron carbon
alloys using a cored wire with a filler material.
[0002] The prior art discloses the use of ultra-dispersed modifiers for out-of-furnace treatment
(secondary treatment) of metallurgical melts.
[0003] The efficiency of ultra-dispersed modifiers largely depends on their morphological
parameters, reactivity and the conditions under which melts undergo modification.
The chief advantage of such modifiers is the large amount of particles per unit volume
in the melt, which essentially determines the efficiency of structure refinement and,
subsequently, leads to a substantial improvement in the mechanical strength and operational
properties of cast products.
[0004] There is a modifier used for treating metallurgical melts known as
RU2651514, IPC C21C1/00, C21C7/00, B82Y30/0, published on April 19, 2018. It contains a multi-component filler encased in a hermetically sealed metal sheath
(jacket). The filler is a mixture rendered uniform and coated with surface-active
agents (surfactants); it contains at least two ultra- and/or fine-dispersed powder
metals having particles up to 10 µm chosen from among the group consisting of iron,
nickel, and aluminum, at least one compound of high melting-point metals, chosen from
among metal carbides, metal borides, metal nitrides, and metal silicides with their
particles ranging between 10 and 200 µm and, at least, one fine-dispersed powder chosen
from among the group consisting of Cn fullerene, carbide clusters, silicon carbide,
copper, calcium, barium, and REMs, whereupon compounds of high melting-point metals
are incorporated into the powder metals. High melting-point metals are represented
by molybdenum, vanadium, tungsten, zirconium, niobium, tantalum, chromium or hafnium.
[0005] The disadvantage of the prior art solution is that a filler is encased in a hermetically
sealed metal sheath (jacket) in the form of steel ampoules or capsules. For their
introduction into molten metal the sandwich process, the Inmold Process, the plunging
method, and other well-known techniques are used. The use of a modifier enclosed in
ampoules or capsules and the methods of its introduction into molten metal do not
make it possible for the modifier to penetrate the full depth of the melt and spread
uniformly therein, thus the modifying effect of the modifier is reduced.
[0006] There is a modifier used for treating liquid steel known as
RU2447176, IPC C22C35/0, published on August 20, 2011. It contains the nanodispersed powder of a high melting-point material and the powder
of a protector. The protector is represented by the powder of one or more master alloys
chosen from among the group consisting of ferrosilicon, ferromanganese, aluminum ferrosilicon,
calcium silicon, barium silicon, calcium silicon barium.
[0007] The disadvantage of the prior art solution is that the modifier is represented by
briquettes into which mixtures of powders uniform in terms of composition are pressed.
The use of a modifier in the form of briquettes does not make it possible for the
modifier to reach the required depth of penetration of the melt and spread uniformly
therein, thus the modifying effect of the modifier is reduced.
[0008] The main reasons preventing ultra-dispersed modifiers from being used by foundries
on a broad scale are that it is necessary to use additional pieces of equipment and
that modifiers have to undergo preliminary preparation prior to being introduced into
molten metal, inconsistent results brought about by the processes of coagulation of
introduced particles, dissolution and distribution of modifiers throughout the entire
volume of the melt.
[0009] It is received wisdom that the most technologically simple and efficient method of
introducing modifiers into melts treated in out-of-furnace treatment facilities is
the cored wire injection method. Use of ultra-dispersed materials (nanomaterials)
as part of filler materials of cored wires makes it possible for them to reach a predetermined
depth of molten metal thus eliminating the likelihood of their impact on molten metal
prematurely (within its upper layers).
[0010] There is a nanostructured cored wire used for underwater welding known as
RU2539284, IPC B23K35/368, B82B3/00 published on January 20, 2015 20.01.2015. It consists of a metal sheath (jacket) encasing charge materials containing rutile
concentrate, hematite, iron powder, ferromanganese, silicon dioxide, an alkali metal
carbonate and an alkali metal complex fluoride. The surface of the sheath (jacket)
has an inner composite coating in the form of a copper matrix in which the nano-sized
particles of an activating flux are distributed. The flux contains an alkali metal
fluoride.
[0011] Use of the composite coating in the form of a copper matrix makes production of a
cored wire quite expensive. Besides, the electrolytic deposition of copper on the
surface of the sheath (jacket) of a cored wire is an inefficient process as the substance
does not coat the surface uniformly.
[0012] Use of this type of cored wire makes it possible to introduce nano-sized particles
into a weld zone but the composition of this type of cored wire makes it impossible
to use it for treating molten metal in an out-of-furnace treatment facility.
[0013] There is also a cored wire known as
RU2381280, IPC C21C7/00 published on February10, 2010. It contains a powdered/granulated filler material, an inner metal sheath surrounding
the said filler material, and, at least, one thermal barrier layer surrounding the
said inner metal sheath. The thermal barrier layer is made of a material that pyrolyzes
upon contact with a molten metal bath, and a soaking liquid loaded in said thermal
barrier layer. The thermal barrier layer is Kraft paper, aluminized paper, or a multiple
layer comprising at least one strip of Kraft paper and at least one layer of aluminized
paper. The pyrolizing material is covered with a thin metallic sheet which is separate
from the internal metallic liner. The outer metal sheath (jacket) is closed using
a lock seam. The powder or particles of the filler material are compacted or embedded
in a resin; the filler material contains at least one material chosen from among the
group consisting of Ca, Bi, Nb, Mg, CaSi, C, Mn, Si, Cr, Ti, B, S, Se, Te, Pb, CaC
2, Na
2CO
3, CaCO
3, CaO, MgO and REMs.
[0014] The solution described in Patent
RU2381280 has been selected as the closest prior art having the closest combination of features
essential to the invention.
[0015] In the prior arrangement of the cored wire, the thermal barrier layer performs only
one function: it prevents the filler material from entering the melt before the cored
wire reaches a predetermined depth. The thermal barrier layer does not contain substances
or materials that could produce a certain modifying effect on the melt.
[0016] The cored wire is distinctive for that a complex process is employed for it to be
manufactured. A sheath having two metallic sheets separated by a layer of paper that
has to be moistened (soaked with liquid). The two metallic sheets make the cored wire
too stiff and complicate its coiling.
[0017] The idea of the present invention is to introduce an additional layer into a cored
wire that performs not only a function as a thermal barrier layer but also contains
ultra-dispersed substances that a certain modifying effect on the melt.
[0018] The technical problem that underlies the present invention and that is to be solved
is to produce a cored wired with a filler material that has a combination of controllable
properties making it possible to use such cored wire for modifying and microalloying
metallurgical melts and ensure that it can be injected into the molten bath to reach
a predetermined depth.
[0019] What makes it possible to solve the said technical problem is that a cored wire for
modifying molten metal in an out-of-furnace treatment facility has a metal sheath
(jacket) encasing a filler material containing at least one element chosen from among
the group consisting of Ca, Ba, Sr, Mg, Si, Al. In addition, at least one coat of
composite material is applied onto the inner and/or outer surface of the metal sheath
(jacket). The composite material is, in fact, a paintwork material containing high
melting-point ultra-dispersed particles selected from compounds of metal carbides
and/or metal nitrides, and/or metal carbonitrides, and/or metal silicides, and/or
metal borides.
[0020] In addition to the above, the paintwork material is polymer-based and/or alcohol-based.
[0021] The composite material contains a protective material represented by ferroalloys
and/or fluxes.
[0022] The metals included in the high melting- point compounds of said cored wire coats
are represented by titanium, and/or tungsten, and/or magnesium, and/or niobium, and/or
vanadium.
[0023] Coats of the composite material are applied onto the surfaces of the metal sheath
(jacket) uniformly.
[0024] Besides, the filler material may additionally contain at least one component selected
from a group of CaC
2, Na
2CO
3, CaCO
3, SrCO
3, CaO, MgO.
[0025] Application of a composite material to the inner and/or outer surface of the metal
sheath (jacket) makes it possible for the ultra-dispersed substances to be deposited
over the entire length of the cored wire and, as a result, for them to penetrate all
the way through the entire volume of the melt in a uniform manner. It also makes it
possible to calculate the required amount of cored wire to be injected, to prevent
the injected particles from coagulating, to increase the specific surface area of
the modifier coming into contact with the melt, to create additional nucleation sites
for solidification thus facilitating maximum assimilation of the modifier and refining
the structure of the melt being modified.
[0026] Upon entering the melt, the composite material deposited on the inner and/or outer
surface of the metal sheath (jacket) gets pyrolyzed absorbing the energy and chilling
down the microparts of molten metal in which the injected cored wire is getting dissolved.
In the course of this process, the ultra-dispersed particles get released. Further,
it allows more time for the cored wire to get dissolved in the molten metal, thus
making it possible for the filler material and the above ultra-dispersed particles
to reach great depths, which enables maximum assimilation of the filler material and
lower consumption of the cored wire used for modification purposes.
[0027] Use of ultra-dispersed particles in the form of metal carbides, and/or metal borides,
and/or metal silicides, and/or metal nitrides, and/or metal carbonitrides, whose melting
temperatures are higher than that of the molten metal being modified makes it possible
for the particles to spread throughout the entire volume of the molten metal being
modified. As a result, grain refinement is promoted and occurrence of grains of varying
sizes is prevented, which results in obtaining the final product with consistently
high isotropic physico-mechanical properties.
[0028] Use of the present invention makes it possible to increase the efficiency of the
modifier encapsulated in the cored wire, improve the quality of the molten metal being
modified, and broaden the scope of application of cored wires.
[0029] The ratio between the components of the filler material and the ultra-dispersed particles
in the coating of the metal sheath (jacket) of a cored wire is calculated on a case-by-case
basis depending on the composition of the molten metal being modified, the method
of modification being used, and the preset properties of the final product.
[0030] According to the present invention, a cored wire for treating molten metal in an
out-of-furnace treatment facility consists of a hermetically sealed metal sheath (jacket),
which is predominantly a steel sheath (jacket). The sheath (jacket) is 0.2 - 0.6 mm
thick, and in its predominant embodiment it should be 0.3 - 0.45 mm thick. The edges
of the sheath (jacket) are closed using a lock seam.
[0031] At least one coat of composite material is applied onto the inner and/or outer surface
of the metal sheath (jacket). The coating is a base matrix performing the function
of a bonding substance and containing particles and a protective material. The protective
material introduced into the base matrix makes it possible to eliminate the likelihood
of the ultra-dispersed particles coagulating. It promotes their uniform distribution
within the coating. The base matrix is a paintwork material. The paintwork material
is polymer-based and/or alcohol-based. The composite material contains a protective
material represented by ferroalloys and/or fluxes. The ultra-dispersed particles are
represented by compounds of carbides, and/or borides, and/or silicides, and/or nitrides,
and/or carbonitrides, whose melting temperature exceeds 1600 °C; The quantitative
content of the ultra-dispersed particles in the coating is 0.01-0.5 % of the weight
of the molten metal being treated. The metals constituting a part of the above compounds
may be titanium and/or tungsten, and/or silicon, and/or magnesium, and/or vanadium.
The coating should predominantly not exceed 300 µm, and the size of the ultra-dispersed
particles of the coating should range from 1 to 200 mµ (nanometers). In specific embodiments
of the cored wire the coating may exceed 300 µm.
[0032] The composite material applied onto the inner and/or outer surface of the metal sheath
(jacket) of a cored wire is a thermal barrier layer containing modifying particles.
[0033] Inside the metal sheath (jacket) of a cored wire there is a multi-component filler
material containing at least one element chosen from among the group consisting of
Ca, Ba, Sr, Mg, Si, Al.
[0034] One of the specific embodiments of the filler material has the following components
in terms of their percentages by weight: barium - 0.001-35, calcium - 0.001-35, strontium
- 0.001-35, magnesium - 0.001-50, silicon - 25-75, TRE - 0.001 - 15, iron - the balance.
[0035] Besides, the filler material may additionally contain at least one component selected
from a group of CaC
2, Na
2CO
3, CaCO
3, SrCO
3, CaO, MgO.
[0036] The filler material is represented by the above substances, for example, in powder
or granular form with their particles not exceeding 3 mm in size.
[0037] The technical character of our invention is illustrated by examples of how the cored
wire having the alleged composition was used for modifying liquid steel and iron.
Example 1.
[0038] In an electric arc furnace, steel 20GFL was melted. It had the following base components
in terms of their percentages by weight:
Ca - 0.16-0.25,
Si - 0.20-0.50,
Mn - 0.90-1.40.
V - 0.06-0.12,
P up to 0.05,
S up to 0.05,
Fe being the balance;
the melt was tapped into two 10-t ladles.
[0039] In ladle # 1, for the purpose of refining and modifying the molten metal, a cored
wire was used 14 mm in diameter with its metal sheath (jacket) being 0.40 mm thick.
It had the following components in terms of their percentages by weight: Si - 43-51,
Ca - 18-22, Ba - 10-15, Sr - 10-15, its core ratio being 0.55. The inner surface of
the metal sheath (jacket) had a paintwork-based coating applied to it. It had a modifying
ultra-dispersed element, TiC
0.4N
0.6 (titanium carbonitride) with its particles being less than 5 mµ in size making up
20 % of the total and a slag-forming mixture, CaO+CaF
2 (calcium oxide + calcium fluoride) with its particles being less than 100 µm making
up 80% of the total. The coat applied is 150-200 µm thick. The amount of the coat
applied ensures that one meter of the cored wire contain at least 10 g of titanium
carbonitride. A total of 5 kg of cored wire was consumed per one ton of molten metal.
[0040] In ladle # 2, for the purpose of modifying the molten metal, a cored wire containing
silicon calcium (SiCa40) was used.
[0041] As the properties of the melt modified with the cored wire having the alleged composition
and those of the melt modified with the cored wire containing silicon calcium (SiCa40)
were compared, the following results were obtained.
[0042] Use of the cored wire having the alleged composition made it possible to reduce the
size of the grain by 24 %, increase the microhardness by 7.4 % and improve KCV impact
toughness at -60 °C of the modified melt by 49%. It also became possible to reduce
the content of non-metallic inclusions.
[0043] Use of the cored wire having the above composition made it possible to improve the
strength, ductility and impact toughness of the modified melt.
Example 2.
[0044] In an electric arc furnace, steel 20GFL was melted. It had the following base components
in terms of their percentages by weight:
Ca 0.16 - 0.25,
Si 0.20-0.50.
Mn 0.90 - 1.40.
V 0.06 - 0.12,
P up to 0.05,
S up to 0.05,
Fe being the balance,
the melt was tapped into two 10-t ladles.
[0045] In ladle # 1, for the purpose of refining and modifying the molten metal, a cored
wire was used 14 mm in diameter with its metal sheath (jacket) being 0.40 mm thick.
It had the following components in terms of their percentages by weight: Si - 43-51,
Ca - 18-22, Ba - 10-15, Sr - 10-15, its core ratio being 0.55. The inner surface of
the metal sheath (jacket) had a paintwork-based coating applied to it. It had a modifying
ultra-dispersed element, 70%TiC+30%VC (70% titanium carbide + 30% of vanadium carbide)
with its particles being less than 5 mµ in size making up 20 % of the total, and ground
ferrotitanium (FeTi70) with its particles being less than 100 µm in size making up
30% of the total, and a slag-forming mixture, CaO+CaF
2 (calcium oxide + calcium fluoride) with its particles being less than 100 µm making
up 50% of the total. The coat applied was 150-200 µm thick. The amount of the coat
applied ensured that one meter of the cored wire contain at least 15 g of titanium
carbide and vanadium carbide. A total of 5 kg of cored wire was consumed per one ton
of molten metal.
[0046] In ladle # 2, for the purpose of modifying the molten metal, a cored wire containing
silicon calcium (SiCa40) was used.
[0047] As the properties of the melt modified with the cored wire having the alleged composition
and those of the melt modified with the cored wire containing silicon calcium (SiCa40)
were compared, the following results were obtained.
[0048] Use of the cored wire having the alleged composition made it possible to reduce the
size of the grain by 29 %, increase the microhardness by 8.1 % and improve KCV impact
toughness at -60 °C of the modified melt by 52%. It also became possible to reduce
the content of non-metallic inclusions.
Example 3.
[0049] In an induction furnace, grey iron (SCh25) was melted. It had the following base
components in terms of their percentages by weight:
Ca 3.20 - 3.40,
Si 1.40 - 2.20,
Mn 0.70 - 1.00,
P up to 0.20,
S up to 0.15,
Fe being the balance,
the melt was tapped into two 5-t ladles.
[0050] In ladle # 1, for the purpose of refining and modifying the molten metal, a cored
wire was used 14 mm in diameter with its metal sheath (jacket) being 0.40 mm thick.
It had the following components in terms of their percentages by weight: Si - 65-75,
Ca - 0.80-1.5, Ba - 3.5-5.00, Al - 1.00-2.00, its core ratio being 0.5. The inner
surface of the metal sheath (jacket) had an alcohol-based coating applied to it. It
had the following modifying elements: SiC+Si
3N
4 (silicon carbide + silicon nitride) with its particles being less than 5 mµ in size
making up 20 % of the total and ground, finely dispersed ferrosilicon with magnesium
and barium with its particles being less than 100 µm making up 80% of the total. The
coat applied is 150-200 µm thick. The amount of the coat applied ensured that one
meter of the cored wire contain at least 15 g of a mixture of carbides and nitrides.
A total of 5 kg of cored wire was consumed per one ton of molten metal.
[0051] In ladle # 2, for the purpose of modifying the molten metal, a cored wire containing
ferrosilicon (FeSi75) was used.
[0052] As the properties of the melt modified with the cored wire having the alleged composition
and those of the melt modified with the cored wire containing ferrosilicon (FeSi75)
were compared, the following results were obtained.
[0053] Use of the cored wire having the alleged composition made it possible to increase
the yield strength by 10.3% and the tensile strength by 12.1%. It also became possible
to improve the wear resistance of the resultant castings.
[0054] The cored wire with the alleged composition may be manufactured as follows. A metal
strip between 0.2 and 0.6 mm thick is roll formed into a cylinder-shaped sheath, or
jacket, having a trough like configuration. A preliminarily prepared powdered filler
material is fed into the sheath (jacket) from a hopper bin and distributed uniformly
along its length. A composite coating is applied to the inner and/or outer surface
of the sheath (jacket) before or after the roll forming process and before the sheath
(jacket) is filled with the filler material. The coating is applied to the inner and/or
outer surface of the sheath (jacket) by spraying or by sprinkling or by means of rollers.
After the sheath (jacket) is filled with the filler material, the sheath (jacket)
is further roll formed to close around the filler material and form a continuous lock
seam. The cored wire thus produced is packaged in coils.
[0055] Cored wires are injected into molten metal using injection machines at speeds ranging
from 35 to 300 m/min. Consumption of cored wire is calculated based on the rate of
consumption of filler material equaling 1.5-7.0 kg per ton of molten metal.
[0056] The present cored wire for out-of-furnace treatment (secondary treatment) metallurgical
melts is distinguished by the great reliability in how it functions and ease of manufacture;
it can be manufactured using familiar equipment, materials and techniques.
[0057] The terms and word combinations used in this description such as "contains", "containing",
"in the predominant embodiment", "predominantly", "in particular", "may be" should
not be interpreted as excluding the presence of other materials, parts, structural
elements, actions.
1. A cored wire intended for out-of-furnace treatment of metallurgical melts has a steel
sheath (jacket) that encases a filler material containing at least one element chosen
from among the group of Ca, Ba, Sr, Mg, Si, Al, in addition, at least one coat of
composite material is applied onto the inner and/or outer surface of the sheath (jacket),
that is in fact a paintwork material containing ultradispersed particles selected
from compounds of metal carbides and/or metal nitrides, and/or metal carbonitrides,
and/or metal silicides, and/or metal borides.
2. The cored wire according to claim 1 wherein the paintwork material is polymer-based
and/or alcohol-based.
3. The cored wire according to claim 1 wherein the composite material contains a protective
material represented by ferroalloys and/or fluxes.
4. The cored wire according to claim 1 wherein the metals contained in the compounds
are represented by titanium, and/or tungsten, and/or silicon, and/or magnesium, and/or
niobium, and/or vanadium.
5. The cored wire according to claim 1 wherein coats of the composite material are applied
onto the surfaces of the sheath (jacket) uniformly.
6. The cored wire according to claim 1 wherein the filler material additionally contains
at least one component chosen from among the group of CaC2, Na2CO3, CaCO3, SrCO3, CaO, MgO.
Amended claims under Art. 19.1 PCT
1. A cored wire intended for out-of-furnace treatment of metallurgical melts has a steel
sheath that encases a filler material containing at least one element chosen from
among the group of Ca, Ba, Sr, Mg, Si, Al, in addition, at least one layer of composite
coating is applied onto the inner and/or outer surface of the sheath, that is in fact
a paintwork material containing ultrafine particles selected from compounds of metal
carbides and/or metal nitrides, and/or metal carbonitrides, and/or metal silicides,
and/or metal borides.
2. The cored wire according to claim 1 wherein the paintwork material is polymer-based
and/or alcohol-based.
3. The cored wire according to claim 1 wherein the composite coating contains a protective
material represented by ferroalloys and/or fluxes.
4. The cored wire according to claim 1 where in the metals contained in the compounds
are represented by titanium, and/or tungsten, and/or silicon, and/or magnesium, and/or
niobium, and/or vanadium.
5. The cored wire according to claim 1 wherein layers of the composite coating are applied
onto the surfaces of the sheath uniformly.
6. The cored wire according to claim 1 wherein the filler material additionally contains
at least one component chosen from among the group of CaC2, Na2CO3, CaCO3, SrCO3, CaO, MgO.